FDA Inspection 1171003 — ADMI

ADMI — FEI 3010057321

The FDA completed an inspection of ADMI on Jun 3, 2022 in East Syracuse, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 3, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
East Syracuse, NY (United States)

Citations

IDCFRDescription
314921 CFR 820.180Availability
316021 CFR 820.184Lack of or inadequate DHR procedures
322621 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.